Hello everyone,
I am using DIA-NN to analyze ultralow sample data acquired with diaPASEF and VistaScan modes from timsTOF Ultra 2.
Multiple peptides of interest fall outside of the fragmentation window and reside in MS1 only.
I was wondering if there are any suggestions on increasing the detection capabilities for these peptides through DIANN instead of running a new acqusition?
Thank you!
While in theory it is possible to identify peptides based on MS1 signal only, this is not currently supported in DIA-NN, i.e. only peptides that are being fragmented will be identified.
Hello everyone, I am using DIA-NN to analyze ultralow sample data acquired with diaPASEF and VistaScan modes from timsTOF Ultra 2. Multiple peptides of interest fall outside of the fragmentation window and reside in MS1 only. I was wondering if there are any suggestions on increasing the detection capabilities for these peptides through DIANN instead of running a new acqusition? Thank you!